Opportunity Description
Job Description:
The Senior CQV Engineer is responsible for leading and executing Commissioning, Qualification, and Validation (CQV) activities with a strong focus on CIP (Clean-In-Place) systems supporting Drug Substance Manufacturing. This role will serve as a technical subject matter expert for CIP system qualification and cleaning validation, ensuring compliance with GMP, regulatory, and internal quality standards.
The ideal candidate brings hands-on experience in CIP system design review, qualification execution, and cleaning validation strategy, and can work independently in a fast-paced manufacturing environment while collaborating cross-functionally with Engineering, Manufacturing, Quality, and Automation teams. Senior CQV Engineer Responsibilities:
CQV & Validation Execution: Lead and execute commissioning, qualification, and validation activities for CIP systems supporting Drug Substance manufacturing operati...
Full-time
Engineers